Oxidation Behavior of CuZr-Based Glassy Alloys at 400 °C to 500 °C in Dry Air

The oxidation behavior of the Cu_47.5Zr_47.5Al₅ (Cu3) and Cu₄₇Ti₃₄Zr₁₁Ni₈ (Cu4) bulk metallic glasses (BMGs) was studied over the temperature range of 400 °C to 500 °C in dry air. The oxidation kinetics of both alloys generally followed a multistage parabolic-rate law, and the steady-state parabolic-rate constants (k _p values) fluctuated with temperature for the Cu3 BMG, but increased with increasing temperature for the Cu4 BMG. The scales formed on the BMGs were strongly dependent on the temperature and alloy composition, and were composed primarily of tetragonal-ZrO₂ (t-ZrO₂) and minor amounts of Al₂O₃, Cu₂O, and CuO at 400 °C for the Cu3 BMG, while the monoclinic-ZrO₂ (m-ZrO₂) phase is present at T ≥ 425 °C, and the Cu₂O phase is absent at 500 °C. Conversely, the scales formed on the Cu4 BMG consisted exclusively of CuO at 400 °C, while minor amounts of t-ZrO₂, TiO₂, and ZrTiO₄ formed at 425 °C to 450 °C, and TiO was also detected at higher temperatures. It was found that both amorphous Cu3 and Cu4 substrates transformed into different crystalline phases, and were strongly dependent on temperature and duration of time. This article is based on a presentation given in the symposium entitled “Bulk Metallic Glasses IV,” which occurred during the TMS Annual Meeting February 25–March 1, 2007, in Orlando, Florida under the auspices of the TMS/ASM Mechanical Behavior of Materials Committee.     

A non-ideal model for predicting the effect of dissolved salt on the flash point of solvent mixtures

Flash point is one of the major quantities used to characterize the fire and explosion hazard of liquids. Herein, a liquid with dissolved salt is presented in a salt-distillation process for separating close-boiling or azeotropic systems. The addition of salts to a liquid may reduce fire and explosion hazard. In this study, we have modified a previously proposed model for predicting the flash point of miscible mixtures to extend its application to solvent/salt mixtures. This modified model was verified by comparison with the experimental data for organic solvent/salt and aqueous-organic solvent/salt mixtures to confirm its efficacy in terms of prediction of the flash points of these mixtures. The experimental results confirm marked increases in liquid flash point increment with addition of inorganic salts relative to supplementation with equivalent quantities of water. Based on this evidence, it appears reasonable to suggest potential application for the model in assessment of the fire and explosion hazard for solvent/salt mixtures and, further, that addition of inorganic salts may prove useful for hazard reduction in flammable liquids.     

<Emphasis Type="Italic">In-Situ</Emphasis> Electrochemical Investigations of a Nickel-Based Alloy Subjected to Fatigue

The HASTELLOY C2000 superalloy is a commercially designed superalloy manufactured to function in reducing and oxidizing corrosive solutions. The industrial applications have tremendous potential in automotive, structural, aviation, and storage components. Although C2000 demonstrates good reducing and oxidizing traits in extremely aggressive media (which are attractive features of its chemistry), changes in the mechanical properties are believed to be insignificant due to its strong propensity to passivate under corrosive conditions. The ductility behavior and corrosion properties of C2000 are superior to those of stainless steels. The objective of the present study is to examine the corrosion-fatigue behavior of C2000 in a 3.5 wt pct sodium-chloride (NaCl) solution. C2000 submerged in 3.5 wt pct NaCl at room temperature is not susceptible to localized corrosion, such as pitting, during fatigue. At an accelerated potential of 350 mV, the current responses show an increase in the current due to slip steps emerging to the surface as a result of fatigue. The crack-initiation site and the examination of the fracture morphology are discussed. This article is based on a presentation given in the symposium entitled “Deformation and Fracture from Nano to Macro: A Symposium Honoring W.W. Gerberich’s 70th Birthday,” which occurred during the TMS Annual Meeting, March 12–16, 2006 in San Antonio, Texas and was sponsored by the Mechanical Behavior of Materials and Nanomechanical Behavior Committees of TMS.

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Radical polymerization of methacryloyl isocyanate containing 1-adamantanol

Summary Radical polymerization of the methacryloyl isocyanate containing 1-adamantanol (Ad-MAI) with AIBN in different solvents at 60°C was investigated. It is observed that polymerization is slower in polar solvents than in nonpolar ones. The rate of polymerization for Ad-MAI was found to be slower than those of Adph-MAI and MMA both in photopolymerization and in thermal polymerization. Copolymerization of Ad-MAI (M₁) with styrene (M₂) in benzene was studied at 60°C. The monomer reactivity ratio was calculated to be r₁=1.53 and r₂=0.76 according to the method of Fineman-Ross. The prominent glass transition temperature for poly(Ad-MAI) was observed at 142°C from global TSC spectrum. Received: 20 November 1998/Revised version: 16 February 1999/Accepted: 25 February 1999     

Surface Graft Copolymerization of Poly(vinylidene fluoride) Film with Simultaneous Lamination to Copper Foil

Surface thermal graft copolymerization with concurrent lamination was carried out between an Ar plasma pretreated poly(vinyh'dene fluoride) (PVDF) film and a copper foil in the presence of a small quantity of a N-containing monomer, such as 4-vinyl pyridine (4-VPN) and acryloyl morpholine (ACMO), under atmospheric conditions and in the complete absence of an added polymerization initiator and system degassing. The adhesion strength, as reported by T-peel strength, was dependent on the argon plasma pretreatment time of the PVDF film, the thermal lamination temperature and the type of monomer. An optimum T-peel adhesion of about 10 N/cm was readily achieved in the Cu/PVDF laminate for grafting and lamination carried out in the presence of 4-VPN. A lower adhesion strength was obtained using ACMO and other N-containing monomers. The chemical compositions of the graft copolymerized and delaminated sample surfaces were studied by X-ray photoelectron spectroscopy (XPS). The failure mode of the Cu/4-VPN/PVDF assembly was a combined adhesional and cohesive failure. The strong adhesion between the Cu foil and the PVDF film arises from the strong charge transfer interaction between Cu and the pyridine ring, as well as the fact that the graft chains are covalently tethered on the PVDF films surfaces as a result of surface graft copolymerization.     

Dilute solution properties of anionic poly(potassium-2-sulfopropylmethacrylate)

The dilute solution properties of an anionic polyelectrolyte, poly(potassium-2-sulfopropylmethacrylate) [poly(SPM)], are studied by measurements of polymerization rate, intrinsic viscosity, degree of binding, ionic strength, and critical micelle concentration. The polymerization of SPM in 0.5M NaCl aqueous solution proceeded more easily than that of SPM in pure water. The polymerization rate of SPM is found to pass through an extreme value as a function of pH. The intrinsic viscosity of this polyelectrolyte is related to the type and concentration of the salt added. The intrinsic viscosity for anionic polyelectrolyte resulting from the electrostatic repulsive force of the polymer chain is in contrast with the polyampholyte. The polyelectrolyte in a high concentration of NaCl has a low degree of binding, indicating that the proton ion (H⁺) is relatively difficult to bind to the sulfonate group (SO⁻₃) at the polymer end. An increase in ionic strength causes the pKa (dissociation constant) to decrease at the half-neutralization point. The monomer solutions exhibit a plot typical of those observed for detergents, with a break in the curve occurring at the critical micelle concentration. For the polymer solutions, no break in the equivalent conductance curve was found for the concentrations studied. The polymer is adapted for use as viscosity-controlling agents in secondary oil recovery operations by water flooding. We have the proposed models to account for the poly(SPM) solution viscometrics. © 1997 John Wiley & Sons, Inc.     

Development of an amperometric ethanol biosensor based on a multiwalled carbon nanotube-Nafion-alcohol dehydrogenase nanobiocomposite

An amperometric biosensor for the determination of ethanol has been constructed. It comprises a multiwalled carbon nanotubes (MWNTs) conduit, a Nafion binder, and an alcohol dehydrogenase (ADH) function. The measurement of ethanol is based on the signal produced by beta-nicotinamide adenine dinucleotide (NADH), the product of the enzymatic reaction. The MWNTs are cylindrical with an outer diameter in the range 40-60 nm, an inner diameter in the range 2-5 nm, and a length of up to several micrometers. The homogeneity of the resulting nanobiocomposite film was characterized by field emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM). The performance of the MWNTs-Nafion-ADH nanobiocomposite modified glassy carbon electrode was examined using cyclic voltammetry and amperometry in presence of NADH and in the presence of ethanol. The electrocatalytic activity of MWNTs towards the oxidation of NADH has allowed an effective low-potential amperometric determination of ethanol. In the case of 6 mgmL(-1) ADH, the MWNTs-Nafion-ADH nanobiocomposite film displayed a sensitivity of 830 nAmM(-1), a linear range up to 0.1 mM, a detection limit of 3 microM, and a response time of about 4 s.     

Neuronal growth cones respond to laser-induced axonal damage

Although it is well known that damage to neurons results in release of substances that inhibit axonal growth, release of chemical signals from damaged axons that attract axon growth cones has not been observed. In this study, a 532 nm 12 ns laser was focused to a diffraction-limited spot to produce site-specific damage to single goldfish axons in vitro. The axons underwent a localized decrease in thickness (‘thinning’) within seconds. Analysis by fluorescence and transmission electron microscopy indicated that there was no gross rupture of the cell membrane. Mitochondrial transport along the axonal cytoskeleton immediately stopped at the damage site, but recovered over several minutes. Within seconds of damage nearby growth cones extended filopodia towards the injury and were often observed to contact the damaged site. Turning of the growth cone towards the injured axon also was observed. Repair of the laser-induced damage was evidenced by recovery of the axon thickness as well as restoration of mitochondrial movement. We describe a new process of growth cone response to damaged axons. This has been possible through the interface of optics (laser subcellular surgery), fluorescence and electron microscopy, and a goldfish retinal ganglion cell culture model.     

Airside performance of herringbone wavy fin-and-tube heat exchangers – data with larger diameter tube

This study examines the airside performance of the wavy fin-and-tube heat exchangers having a larger diameter tube (D_c = 16.59 mm) with the tube row ranging from 1 to 16. It is found that the effect of tube row on the heat transfer performance is quite significant, and the heat transfer performance deteriorates with the rise of tube row. The performance drop is especially pronounced at the low Reynolds number region. Actually more than 85% drop of heat transfer performance is seen for F_p ～ 1.7 mm as the row number is increased from 1 to 16. Upon the influence of tube row on the frictional performance, an unexpected row dependence of the friction factor is encountered. The effect of fin pitch on the airside performance is comparatively small for N = 1 or N = 2. However, a notable drop of heat transfer performance is seen when the number of tube row is increased, and normally higher heat transfer and frictional performance is associated with that of the larger fin pitch.